ClinVar for MedGen (Select 9033) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 813262	Single allele	CFH, KCNT2	Deletion	Mesangiocapillary glomerulonephritis	GLikely pathogenic
Select item 812882	NM_000064.4(C3):c.3085G>A (p.Asp1029Asn)	C3 (D1029N)	Single nucleotide variant (missense variant)	Mesangiocapillary glomerulonephritis	GLikely pathogenic